Medical Manager

Overview

I am currently hiring for an international specialty pharmaceutical organisation advancing innovative treatments. I am looking for a Medical Manager to provide scientific and medical leadership across clinical programs, ensuring high‑quality study design, execution and oversight.

• Lead medical oversight for clinical studies, including protocol development and Quality‑by‑Design principles.
• Act as medical monitor: safety review, medical queries, oversight of study conduct.
• Support development of CRFs, Medical Monitoring Plans, and Clinical Study Reports.
• Maintain strong relationships with investigators and clinical sites.
• Provide medical input to pharmacovigilance activities for clinical and post‑authorisation studies.
• Review clinical and safety data; identify risks and propose solutions.
• Ensure inspection readiness and support GCP audits/inspections.
• Contribute to process improvements, digital trial initiatives, and cross‑functional knowledge transfer.
• Provide internal scientific training and represent the organisation at scientific meetings.
• Support communication with regulatory authorities as required.

• MD (or equivalent) from UK, EU, or USA.
• 3+ years' experience in clinical research/clinical development.
• Strong knowledge of ICH/GCP and global clinical trial regulations.
• Experience in medical monitoring, protocol development, and clinical data review.
• Excellent written and verbal communication skills.
• Strong analytical, decision‑making, and project leadership abilities.
• Ability to work independently, manage deadlines, and solve problems quickly.

• Competitive salary and benefits.
• Opportunity to impact patient care and contribute to meaningful scientific progress.
• High exposure to senior scientific experts and strategic programs.
• Collaborative, intellectually driven environment focused on clinical excellence.
• Hybrid work model with two days on‑site.

• Medical Doctor
• Clinical Development
• Clinical Trial Management
• Medical Monitoring
• Protocol Development
• Quality by Design (QbD)
• Pharmacovigilance
• ICH/GCP Compliance
• Clinical Data Review
• Medical Affairs
• Cross‑functional Leadership
• Investigator Engagement
• Clinical Site Management
• Risk Management
• Clinical Project Management
• SOP Development
• Scientific Communication
• Regulatory Interaction
• Inspection Readiness
• Audit Support
• Clinical Strategy
• Medical Governance
• Stakeholder Management
• Scientific Writing
• Problem Solving
• Time Management

If this aligns with your expertise and ambition, I invite you to take the next step and apply.